Rare loss-of-function mutations of <i>PTGIR</i> are enriched in fibromuscular dysplasiaAdrien Georges, Nabila Bouatia‐Naji, Anna Baranowska et al.|Cardiovascular Research|2020Cited by 32
Author Correction: Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseasesAdrien Georges, Michel Azizi, Sergiy Kyryachenko et al.|Nature Communications|2022Cited by 2